{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "91441",
      "recalling_firm": "MACLEODS PHARMA USA, INC",
      "address_1": "103 College Rd E Fl 2",
      "address_2": "N/A",
      "postal_code": "08540-6611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within United States and Puerto Rico.",
      "recall_number": "D-0162-2023",
      "product_description": "Levofloxacin Tablets, USP 500 mg; 50-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540; Manufactured by: Macleods Pharmaceuticals Ltd., Baddi, Himachal Pradesh, India. NDC 33342-022-08",
      "product_quantity": "10052 bottles",
      "reason_for_recall": "Mismatching of the embossing on the tablets (T7) with the embossing mentioned in the package insert (ML63) in the distributed bottles.",
      "recall_initiation_date": "20230105",
      "center_classification_date": "20230117",
      "termination_date": "20250624",
      "report_date": "20230125",
      "code_info": "Lot #: BLF2214A; Exp. 06/2025"
    }
  ]
}